2018
DOI: 10.4274/jtgga.2018.0002
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Association between fok1 polymorphism of vitamin D receptor gene with uterine leiomyoma in Turkish populations

Abstract: Objective:The aim of this research was to determine the association between the fok1 polymorphism and uterine leiomyomas.Material and Methods:For genotyping the fok1 polymorphism of the vitamin D receptor, real-time polymerase chain reaction was performed on blood samples of uterine leiomyoma (n=27) and control (n=33) groups. For statistical analyses, SPSS v.23 software (SPSS Inc., Chicago, IL, USA) was used.Results:A statistically significant difference was observed for the frequency of the CC genotype betwee… Show more

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Cited by 10 publications
(8 citation statements)
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“…Despite the positive results regarding the increased risk for UFs in the selected VDR polymorphisms obtained by Shahbazi [ 15 ] and Gulec Yilmaz et al [ 33 ], our larger sample size study did not confirm these findings. The difference may have resulted from the ethnicity of the investigated populations.…”
Section: Discussioncontrasting
confidence: 90%
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“…Despite the positive results regarding the increased risk for UFs in the selected VDR polymorphisms obtained by Shahbazi [ 15 ] and Gulec Yilmaz et al [ 33 ], our larger sample size study did not confirm these findings. The difference may have resulted from the ethnicity of the investigated populations.…”
Section: Discussioncontrasting
confidence: 90%
“…On the other hand, Anderson et al found an association between rs2228570 and reduced risk of breast cancer [ 57 ]. Finally, in his recent publication, Shahbazi found that rs2228570 was associated with UF development in Iranian women [ 15 ], which is consistent with the recent analysis performed on Turkish women [ 33 ]. Moreover, the importance of rs2228570 polymorphism has been shown in Saudi breast cancer patients [ 58 ].…”
Section: Discussionsupporting
confidence: 81%
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“…The study by Shahbazi et al supports the hypothesis that UFs are associated with the VDR rs2228570 polymorphism—correlation between VDR TT genotype and UF occurrence risk [ 121 ]. More recently (2018), Yilmaz et al demonstrated that the presence of the rs2228570 CC genotype may be a risk-reducing factor and the T allele may be a potential risk factor for the development of UFs, which is consistent with the findings of Shahbazi [ 122 ]. Both studies had limitations: small sample size and closed populations and their results need to be confirmed on larger populations [ 120 ].…”
Section: Discussionsupporting
confidence: 62%
“…Recently, several genetic mutations have been known in the vitamin D receptor (VDR). One of them, among many others, is the Fok1 single nucleotide polymorphism that has been linked to gynecological disorders as uterine leiomyoma and polycystic ovary (26,27). Hussain et al according to a study on 340 female students from the Dubai Medical University reported that the frequency of F-containing genotypes between VDR Fok1 genotypes (FF, Ff, and ff) was significantly higher among the PMS group (56.8%) than the control group (44.1%).…”
Section: Discussionmentioning
confidence: 99%